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clinical dysmorphology

ISSN 1473-5717· EN

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About This Journal

Short Name clin dysmorphol
Abbreviated Name clin dysmorphol
ISSN 1473-5717

Publications Per Year

Articles (1)

2020
A novel mutation which causes a frameshift in the PHOX2B gene causes Haddad syndrome.
359 views DOI
2020
A novel mutation which causes a frameshift in the PHOX2B gene causes Haddad syndrome.
359 views DOI
Journament Score

Not calculated yet. A score appears once enough articles and journal metadata have been indexed.